Aromatic polymers of increased resistance to flow and molecular weight obtained by irradiation

ABSTRACT

Aromatic polymers of increased resistance to flow and molecular weight are obtained by irradiation using β-rays or γ-rays at temperatures up to 400°C of an aromatic polymer whose molecular chains comprise benzenoid groups and bivalent linking groups, and where irradiation is γ-rays by heating subsequent to irradiaton at 200°C to 400°C. The polymeric materials having increased molecular weight are useful for coating non-cooking surfaces of cookware.

This application is a Continuation-in-part application of U.S. Application Ser. No. 381 382 filed July 23, 1973 which is a Continuation-in-part Application of U.S. Application Ser. No. 207 948 filed Dec. 14, 1971 and now abandoned.

This invention relates to aromatic polymers of increased molecular weight.

In an article by A. Davis, M. H. Gleaves, J. H. Golden and M. B. Huglin in Die Makromoleculaire Chemie (1969), volume 129 pages 63 to 72, aromatic polysulphone having repeating units of the formula ##SPC1##

Is said to have remarkable stability to electron beam irradiation at ambient temperature in vacuum and in air. Doses of up to 80 Mrads appear to have little effect and higher doses up to 400 Mrads are said to produce chain scission as well as cross-linking. Mechanical properties such as yield strength are said to show no change up to 200 Mrad dose and elongation at break appears constant up to 100 Mrads and decreases slightly between 100 Mrads and 200 Mrads. The mechanism of radiation chemistry is discussed and thought to be mainly through initial hydrogen abstraction from the isopropylidene group.

An article by J. R. Brown and J. H. O'Donnell in Polymer Letters 1970 volume 8 pages 121 - 126 describes irradiation of aromatic polysulphone with γ-radiation and concluded that the radiation stability thereof was the highest reported for any organic polymer. They found that there was a small net rate of degradation on irradiation in air and of cross-linking in vacuum.

It is therefore surprising that irradiation in air with electron-beam/β-ray at low doses leads to an increase in molecular weight and in profound modification in polymer properties such as increased resistance to flow often accompanied by increase in tensile break strength and yield strength.

According to the present invention, aromatic polymers having increased molecular weight and resistance to flow are produced by the exposure to a total dose of 10 to 150 Mrads of ionizing radiation selected from electron beam and β-ray at temperatures of 100°C to 400°C of at least one aromatic polysulphone containing repeat units --Ar-SO₂ -- (where Ar is a bivalent aromatic residue which may vary from unit to unit in the polymer chain and at least some of the Ar units have an aromatic ether or thioether group in the polymer chain ortho or para to at least one --SO₂ -- group). Low doses of electron beam/β-ray radiation may increase the molecular weight of the polysulphone while leaving it thermoplastic; the higher doses result in cross-linking of the polymer chains so that the polymer becomes insoluble in solvents and is no longer thermoplastic. The effect of irradiation is enhanced if the irradiated aromatic polysulphone is heated after irradiation at temperatures of 200°C to 400°C.

Aromatic polymers having increased molecular weight and resistance to flow are also produced by irradiation with γ-rays at temperatures up to 400°C followed by heating at 200°C to 400°C.

Post irradiation heating is essential where radiation is other than electron beam/β-ray because radiation other than those is usually available only at low dose rates. Where radiation is electron beam/β-ray, post-irradiation heating is not essential but may be desirable to increase the effect of irradiation or to produce a required amount of cross-linking from a lower dose of radiation.

Aromatic polysulphones and methods for making them, are described in British Patent Specifications Nos. 1,016,245; 1,060,546; 1,078,234; 1,109,842; 1,122,192; 1,133,561; 1,153,035; 1,153,528; 1,177,183, and 1,234,301, United States Specification No. 3,432,468, Netherlands Specifications Nos. 69 03,070 and 70 11,346 and German Specification No. 1,938,806, the disclosures of which are incorpoated herein by reference.

The aromatic polysulphones described in the above-mentioned specifications comprise repeating units of the formula

    --Ar-SO.sub.2 --

in which Ar is a bivalent aromatic radical and may vary from unit to unit in the polymer chain (so as to form copolymers of various kinds). Thermoplastic polysulphones generally have at least some units of the structure ##SPC2##

in which Y is oxygen or sulphur or the residue of an aromatic diol such as 4,4'-bisphenol. One example of such a polysulphone which is commercially available (Imperial Chemical Industries Limited) has repeating units of the formula ##SPC3##

another has repeating units of the formula ##SPC4##

and others (which are also commercially available) are said to have repeating units of the formula ##SPC5##

(Union Carbide Corporation) or copolymerised units in various proportions of the formulae ##SPC6##

(Minnesota Mining and Manufacturing Company). Another group of aromatic polysulphones has repeating units of the formula ##SPC7##

(where Z is oxygen or sulphur), and these may also be copolymerised with units of other formula given above.

The polymers of increased molecular weight and resistance to flow according to the invention are therefore prepared by irradiating the aromatic polysulphone with electron beam/β-ray ionizing radiation or with γ-ray followed by post-irradiation heating. Preferred radiation is electron beam which is produced for example by accelerators or linear accelerators. Electron accelerators having arc voltages of between 100 kev and 4 Mev are preferred. The aromatic polysulphone may be irradiated in air, in an inert atmosphere for example nitrogen or in vacuo although for industrial applications irradiation in air is more attractive. The dose of the radiation required to increase the molecular weight of the aromatic polymer depends on a number of factors such as the temperature at which irradiation is carried out, the form of aromatic polymer, and the susceptibility of the aromatic polymer to cross-linking and the presence of any cross-linking agents and whether the irradiation is carried out in air or a partial vacuum. For example, a film requires less intense radiation for uniform cross-linking than a moulding having appreciable thickness and thus requiring higher intensity radiation for appreciable penetration. Because a cross-linked aromatic polymer is essentially non-thermoplastic, it is convenient to form the aromatic polymer into the required shape before radiation.

If, however, where ionizing radiation is electron beam/β-rays and the radiation dose is not sufficient to effect cross-linking of the polymer, there will still be an increase in the molecular weight and resistance to flow of the polymer, which remains thermoplastic. Such a dose might be for example 25 M Rads at 100°C. Subsequent heating up to a temperature of 400°C for up to 36 hours as hereinbefore described will lead to a further increase in molecular weight. This heating may be carried out on the irradiated product directly or may be part of a thermoforming stage such as for example extrusion and/or moulding.

Cross-linking may be more readily effected if the aromatic polymer is mixed with up to 5% by weight of sulphur as a cross-linking agent, as may be present in a sulphur compound such as for example elemental sulphur, aliphatic and aromatic dithiols, and aliphatic and aromatic polydisulphides; but melt fabrication of such a mixture before irradiation may be hindered by cross-linking promoted by the presence of the sulphur compound. Elemental sulphur up to a concentration of 5% w/w is preferred. Hence for example noticeable cross-linking occurs on exposure of a film having a thickness 25 μm, prepared from a thermoplastic aromatic polysulphone containing 1% w/w elemental sulphur to an electron beam dose of 40 M Rads at 20°C.

The polymers of the invention may be used for example in the preparation of heat resistant films, foams, mouldings, coatings, and heat resistant insulation of electrical conductors. They may be used in laminates in which the polymers form the adhering members and/or the adhesive bonding them.

A foamed product may be prepared if the aromatic polysulphone is mixed with between 1% and 5% by weight of elemental sulphur and the mixture heated and irradiated in the absence of imposed pressure at a temperature between 300°C and 450°C. A foamed product may also be prepared if the aromatic polysulphone is foamed with a conventional blowing or foaming agent, and subsequently irradiated.

According to a further aspect of the present invention coated cookware is provided having a non-cooking surface coated with aromatic polysulphone having molecular weight increased subsequent to coating. The coating on the cookware of the present invention preferably comprises pigmented aromatic polysulphone.

Decorative cookware often comprises a metal dish particularly cast iron coated with an enamel. Such cookware is generally expensive and can be prone to chipping of the enamel. Other decorative cookware comprises heat resistant glass or other vitreous material which is often pigmented, but such cookware is also generally expensive. The present embodiment provides cookware in which conventional cookware is decorated by a comparatively cheap, heat resistant coating. Increasing of molecular weight generally leads to improved resistance to washing-up or dish-washing procedures, and prevents softening and flow of the coating if it should become overheated.

The pigment which is preferably present in the coated cookware of the embodiment of the present invention is any pigment which is stable at the cooking temperature and the temperature at which the aromatic polysulphone is treated after coating, if so treated. Suitable pigments include for example titanium dioxide, carbon black cadmium pigments.

The aromatic polymer, if desired premixed with pigment can be applied to the cookware before irradiation by any one of a variety of methods. The polymer can be applied from solution, optionally containing dispersed pigment and the cookware coated by for example spraying or dipping followed by solvent evaporation. The solvent is preferably one giving a polymer solution having long pot-life: for example mixtures of cyclohexanone (15-20 parts by volume), methyl ethyl ketone (4-7 parts) and dimethyl sulphoxide (1-3 parts) containing 5 to 25 g of polymer in 100 cm³ of solution. The polymer may be coated by fluidized bed techniques or by spraying polymer particles preferably in a gas against the surface to be coated while the surface is above the softening temperature of the polymer. Alternatively a paste of the polymer may be printed onto the surface or part of the surface by printing techniques such as screen printing. Also patterns can be produced by such printing techniques or by selectively etching or dissolving away selected portions of the coating. However if no pigment is present in the initial coating it is essential that pigment be added at some subsequent stage in order to obtain a pigmented patterned surface.

The cookware may be made of metal e.g. iron, aluminium, steel or of ceramic e.g. glass, pottery, porcelain. Examples of cookware are pans and dishes, pressure cookers, frying pans, baking tins, casserole dishes.

The invention is illustrated by the following examples, in which the physical properties of the materials were measured as follows:

Reduced viscosity of the polysulphone was measured on a solution in dimethylformamide at 25°C containing 1 g of polymer in 100 cm³ of solution.

The "cut-through" temperature was determined using an apparatus similar to that of ASTM D1676, in that the apparatus had two electrodes comprising uninsulated tensioned copper wire mounted one above the other and separated by a piece of film under test. The upper electrode was subjected to a 1 kg downward vertical load and the apparatus was placed in an oven with air circulation having a rate of temperature rise of 5° ± 1°C per minute. The temperature at which the film softened sufficiently to allow continuity of circuit between the two electrodes was noted as the "cut-through" temperature.

The "yield strength", "break strength" and "elongation" of the film samples were determined at about 20°C on an "Instron" TM/M tensile tester having a clamp speed of 20 mm/min. and using a film sample 20 mm long and 10 mm wide.

EXAMPLE 1

A sample of polysulphone having repeat units of the formula ##SPC8##

prepared in a manner similar to that described in Example 3 of British Patent Specification No. 1,153,035 and having a reduced viscosity of 0.5 was extruded into film having a thickness of 250 μm using an extruder having screw diameter 40 mm and barrel temperature 350°C.

Portions (A to F) of the film were irradiated with electron beam produced on a linear accelerator having an arc voltage of 4 Mev and providing a dose rate of 3.5 × 10⁶ Rads/min. Portion (G) was not irradiated and served as a control sample and portion (H) was heated for 10 minutes at 280°C but not irradiated. The results shown in the accompanying table show that irradiation produced film having increased resistance to flow, higher cut-through temperature, superior resistance to solvents, and lower elongation at break whilst the yield strength remained essentially unchanged.

                A      B     C     D     E     F      G    H                       Exposure time                                                                              3      5     10    10    10    15     0    0                       (minutes)                                                                      Exposure    295    350   160   275   330   300    --   280                     temperature (°C)                                                        __________________________________________________________________________     Test (after                                                                    irradiation)                                                                             very slight                                                                           very slight                                                                           slight                                                                               slight                                                                               no    no    immediate                      Immersion in                                                                             crazing                                                                               crazing                                                                               crazing                                                                              crazing                                                                              crazing                                                                              crazing                                                                              craze --                       xylene    after 2.5                                                                             after 2.5                                                                             after 1                                                                              after 1                                                                              after after                                          hours  hours  hour  hour  2.5 hrs                                                                              2.5 hrs                              Time to flow                                                                   at 270°C                                                                          >24 hour                                                                              >24 hour                                                                              40 min.                                                                              40 min.                                                                              >24 hour                                                                             >24 hour                                                                             10 min.                                                                              --                       Yield strength                                                                           85     83.5                     88.3  86.4  80.1                     (MN/m.sup.2)                                                                   Break strength                                                                           71.5   69.5                     73.6  68.7  66.7                     (MN/m.sup.2)                                                                   Elongation at                                                                            120    65                       30    160   110                      break (%)                                                                      Thickness (μm)                                                                        54     56                       54    55    62                       Cut-through                                                                              280    290                      300   250                            temperature (°C)                                                        __________________________________________________________________________

EXAMPLE 2

A sample of polysulphone described in Example 1 but having reduced viscosity 0.4 was mixed with elemental sulphur (1% by weight) as powder on a mill at ambient temperature. A portion of the mixture was compression moulded into film having thickness 55 μm by pressing the portion between chromium plated surfaces at 300°C for 5 minutes. The surfaces were then cooled and the film removed.

A piece of the film was irradiated at 20°C by passing the piece eight times across a source of electron beam emitted from a linear accelerator having an arc voltage of 260 kev, a current in the electron beam of 40 mA and a dose rate of 5 M Rads per pass to give a dose of 40 M Rad. The irradiated film flowed after 2.5 hours at 270°C and crazed after 1 hour in xylene, but a non-irradiated film flowed after 10 minutes at 270°C and crazed after 10 seconds in xylene.

EXAMPLE 3

Samples of film were prepared as described in Example 1 except that the polysulphone had reduced viscosity of 0.58. The film was irradiated at 260°C with an electron beam from an accelerator having arc voltage of 500 kev to provide a dose of 40 M Rads.

Results of physical testing are presented in the table below. For determination of water vapour permeability, a piece of film was used as a membrane separating a stream of nitrogen gas having relative humidity of 90% from a stream of dry nitrogen. The system was allowed to reach a steady state and the amount of water absorbed by the dry nitrogen stream through passage of water vapour through the membrane was then measured using an electrolytic hygrometer. The determinations were carried out at 27°C and the water vapour permeability calculated from the amount of water detected, nitrogen gas flow rate, membrane exposure time and thickness and surface area of the membrane.

Water uptake is expressed as percentage increase in weight of the film on immersion in water until constant weight was achieved.

In the strain ageing test, a piece of film was folded through 180° into a loop and clamped so that the distance from the edge of the clamp to the fold was 7 cm.

    __________________________________________________________________________     Property (units)                                                                               Unirradiated Film                                                                             Irradiated Film                                 __________________________________________________________________________     Tensile break Strength                                                          (MN/m.sup.2)                                                                    20°C   71.2           79.6                                             180°C   35.1           50.3                                            Elongation at break                                                               20°C (%)                                                                             103%           49.2                                             180°C    38%           11                                              Tensile strength after                                                                         Film flowed    90.1                                            ageing for 14 days                                                             at 250°C (MN/m.sup.2)                                                   Cut through temperature                                                                        234°C   286°C                                    Ageing under strain at 230°C                                                            Film crazed after 14 days                                                                     Film unchanged                                  Water uptake at 20°C (%)                                                                2.058          1.95%                                           Permeability (mole meter                                                       sec.sup..sup.-1 newton.sup..sup.-1) to water                                                   9.5 × 10.sup..sup.-13                                                                   5.0 × 10.sup..sup.-13                     vapour                                                                         Solvent resistance                                                                             Film crazes immediately                                                                       Slight crazing after                            (a) xylene at 70°C                                                                      when placed in xylene and                                                                     15 mins. No further                                             breaks after 6 hours                                                                          change after 24 hours                           __________________________________________________________________________

Similar results were obtained using film made from "Polysulphone" 1700 (Union Carbide Corporation) believed to have repeating units of the formula ##SPC9##

with a dose of 100 M Rads.

EXAMPLE 4

A piece of polysulphone film was prepared by the method of Example 1 except that the polysulphone had a reduced viscosity of 0.57. Portions of the film were irradiated at room temperature with electron beam from an accelerator having arc voltage of 200 kev. Some of the portions were heated before or after irradiation at 250°C for 16 hours. The tensile properties of films so treated are presented in the following table where it is apparent that irradiation followed by heating is associated with an increase in tensile break strength and a reduction in elongation of the films. The films were also insoluble in dimethyl formamide after heating.

    __________________________________________________________________________                Tensile Yield                                                                            Tensile Break                                                                            Elongation                                      Film Treatment                                                                            Strength (MN/m.sup.2)                                                                    Strength (MN/m.sup.2)                                                                    (%)                                             __________________________________________________________________________     Unirradiated                                                                              72        60        50                                              Irradiated 71        59        88                                              (dose 30 M Rads)                                                               Irradiated 70        58        31                                              (dose 100 M Rads)                                                              Unirradiated and                                                                          Film Flowed                                                         heated at 250°C                                                         Irradiated Did not   131       12                                              (dose 30 M Rads)                                                                          yield                                                               and then heated                                                                Irradiated Did not   146       12                                              (dose 100 M Rads)                                                                         yield                                                               and then heated                                                                __________________________________________________________________________

Similar experiments on a range of polysulphone films made from polysulphones having reduced viscosity 0.4 to 0.58 showed that films having reduced viscosity in the range 0.4 to 0.45 had the greatest resistance to radiation and that doses of up to 120 M Rads gave no detectable cross-linking before further heating. Films from polymer having reduced viscosity greater than 0.45 exhibited slight cross-linking with doses of 70 M Rads at 22°C.

EXAMPLE 5

The procedure of Example 4 was repeated except that "Polysulfone" 1700 (Union Carbide Corporation) was used as the polysulphone and the irradiated film was heated for 28 days at 250°C. The results of physical testing before and after irradiation are given in the following table.

    ______________________________________                                         Film Treatment                                                                              Tensile Yield                                                                             Tensile Break                                                                             Elongation                                               Strength   Strength                                                            (MN/m.sup.2)                                                                              (MN/m.sup.2)                                                                              (%)                                         ______________________________________                                         Unirradiated 69         65         190                                         Irradiated with                                                                             70         60         129                                         dose of 45 M Rads                                                              Irradiated with                                                                             73         63         150                                         dose of 75 M Rads                                                              Unirradiated but                                                                            Film Flowed                                                       heated at 250°C                                                         Irradiated with                                                                             Did not    86         7                                           45 M Rads then                                                                              yield                                                             heated at 250°C                                                         Irradiated with                                                                             Did not    87         6                                           75 M Rads then                                                                              yield                                                             heated at 250°C                                                         ______________________________________                                    

EXAMPLE 6

Samples of film described in Example 4 (using the 0.57 reduced viscosity polysulphone) were irradiated at room temperature with γ-radiation from a Cobalt-60 source. Portions of the samples were heated before or after irradiation at 250°C for 16 hours. The tensile properties of resultant film are presented in the following table where it is apparent that the degree of cross-linking is not so extensive as that induced by β-rays as evidenced by Example 5.

    ______________________________________                                         Film Treatment                                                                              Tensile  Tensile  Elonga-                                                                               Reduced                                               Yield    Break    tion   Viscosity                                             Strength Strength (%)                                                          (MN/m.sup.2)                                                                            (MN/m.sup.2)                                             ______________________________________                                         Unirradiated 80       69       165    0.57                                     Irradiated   73       63       80     0.40                                     (dose 75 M Rads)                                                               Irradiated   70       58       12     0.29                                     (dose 150 M Rads)                                                              Unirradiated and                                                                            Film Flowed                                                       heated at 250°C                                                         Irradiated   Did not  80       12     0.60                                     (dose 75 M Rads)                                                                            yield                                                             and then heated                                                                Irradiated   Did not  88       11     Slight                                   (dose 150 M Rads)                                                                           yield                    gelation                                 and then heated                                                                ______________________________________                                    

The results above agree with the findings described in the Polymer Letters article hereinbefore referred to, in which molecular weight of "Polysulfone" 1700 is apparently reduced by γ-irradiation at room temperature in air.

EXAMPLE 7

The procedure of Example 6 was repeated but using "Polysulfone" 1700 (Union Carbide Corporation) as the polysulphone and the irradiated film was heated after irradiation for 30 minutes at 250°C and then 21 days at 200°C. The results of physical testing before and after irradiation are presented in the following table.

    ______________________________________                                         Film Treatment                                                                            Tensile Yield                                                                             Tensile Break                                                                               Elongation                                             Strength   Strength                                                            (MN/M.sup.2)                                                                              (MN/m.sup.2) %                                           ______________________________________                                         Unirradiated                                                                              69         65           190                                         Irradiated with                                                                           69         67           180                                         20 M Rads                                                                      Irradiated with                                                                           70         56           110                                         50 M Rads                                                                      Unirradiated                                                                              --         56           8                                           then heated                                                                    Irradiated --         76           10                                          20 M Rads then                                                                 heated                                                                         Irradiated --         77           9                                           50 M Rads then                                                                 heated                                                                         ______________________________________                                    

EXAMPLE 8

Polysulphone of Example 1 but having a reduced viscosity of 0.56 and in the form of cylindrical granules (2.4 mm long; 1.6 mm diameter) was irradiated with γ-radiation from a Cobalt-60 source at room temperature with doses up to 75 M Rads. The irradiated polymer was then extruded at 350°C, polymer residence time in the extruder being 80 seconds. Measurements of reduced viscosity presented in the table below show that the extrudate had increased in reduced viscosity on extrusion.

    ______________________________________                                         Irradiation                                                                               Reduced Viscosity                                                                             Reduced Viscosity                                    dose (M Rads)                                                                             of Chip        of Extrudate                                                    after irradiation                                                   ______________________________________                                          0 (control)                                                                              0.56           0.55                                                 20         0.55           0.70                                                 50         0.57           0.76                                                 75         0.57           0.92                                                 ______________________________________                                    

In a similar experiment a sample of granules of "Polysulfone" 1700 (Union Carbide Corporation) believed to have repeating units of the formula ##SPC10##

and having a reduced viscosity of 0.37 was irradiated with γ-radiation (dose 50 Mrads) and then extruded at 350°C with a residence time in the extruder of 80 seconds. The reduced viscosity of the extrudate was 0.43.

EXAMPLE 9

A solution in dimethyl formamide (100 cm³) of aromatic polysulphone (25 g) similar to that described in Example 1 but having reduced viscosity of 0.40 was brushed onto an aluminium pan having depth 10 cm and diameter 20 cm. The aromatic polysulphone was irradiated at room temperature with an electron beam from an accelerator having arc voltage of 500 kev. to give a dose of 100 Mrads. On being heated to 250°C the coating did not flow whereas that of a pan coated similarly but without subsequent irradiation showed polymer flow on being heated to 250°C. The performance of coating could be improved by heating during or subsequent to irradiation. 

We claim:
 1. An aromatic polymer having increased molecular weight and resistance to flow produced by the exposure to a total dose of 10 to 150 Mrads of β-ray ionizing radiation at a temperature of 100°C to 400°C of at least one aromatic polysulphone containing repeat units --Ar-SO₂ -- (where Ar is a bivalent aromatic residue which may vary from unit to unit in the polymer chain and at least some of the Ar units have an aromatic ether or thioether group in the polymer chain ortho or para to at least one --SO₂ -- group).
 2. An aromatic polymer according to claim 1 produced by exposure to a total dose of 25 to 100 Mrads of β-ray ionizing radiation.
 3. An aromatic polymer according to claim 2 which has been heated subsequent to said radiation at a temperature of 250°C to 400°C.
 4. An aromatic polymer, according to claim 1 which contains repeating units of the formula ##SPC11##
 5. An aromatic polymer, according to claim 1 which contains repeating units of the formula ##SPC12##
 6. An aromatic polymer, according to claim 1 in the form of a shaped article.
 7. An aromatic polymer, according to claim 1 in the form of a film.
 8. Cookware having non-cooking surface coated with an aromatic polymer as claimed in claim
 1. 9. Cookware according to claim 1 in which the coating contains a pigment.
 10. A method of forming a cross-linked aromatic polymer comprising exposing at least one aromatic polysulphone containing repeat units --Ar--SO₂ --, where Ar is a bivalent aromatic residue, which may vary from unit to unit in the polymer chain, and at least some of the Ar units have an aromatic ether or thioether group in the polymer chain ortho or para to at least one --SO₂ -- group, to a total dose of 10 to 150 Mrads of β-ray ionizing radiation at a temperature of 100°C to 400°C to effect cross-linking.
 11. A method according to claim 10 wherein the aromatic polysulphone is subjected to a total dose of 25 to 100 Mrads of said ionizing radiation.
 12. A method according to claim 11 wherein the irradiated polymer is subjected to a temperature of 250°C to 400°C.
 13. A method according to claim 10 in which the aromatic polysulphone contains repeating units of the formula ##SPC13##
 14. A method according to claim 10 in which the aromatic polysulphone contains repeating units of the formula ##SPC14##
 15. A method according to claim 10 wherein the irradiated aromatic polysulphone is subjected to a temperature of 200° to 400°C and is fabricated into a shaped article prior to or during the post-irradiation heating step.
 16. A method according to claim 15 wherein the aromatic polysulphone is fabricated into a shaped article prior to the irradiation step. 